Product Recalls in Montana

Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,400 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,400 in last 12 months

Showing 2120121220 of 48,326 recalls

FoodJune 19, 2019· UNFI General Corporate

Recalled Item: WOODSTOCK ORGANIC GRILLED RED PEPPER Recalled by UNFI General Corporate Due...

The Issue: Product tested positive for Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex Med 4" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex NL 3" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex Med 3" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex NL 4" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Elekta, Inc.

Recalled Item: iGUIDE System with software build iGuide 2.2.0 Recalled by Elekta, Inc. Due...

The Issue: Potential for iGUIDE to incorrectly monitor the 3D position.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: ElectroMist product codes: 36-3310-25 - Product Usage: Electrode...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: Alpha Conducting solution product codes: 3310-25 ASCR - Product Usage:...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: ElectroMist product codes: 36-3310-60 - Product Usage: Electrode...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: ElectroMist product codes: 36-3310-04 - Product Usage: Electrode...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: Alpha Conducting solution product codes:3310-15 ACS - Product Usage:...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Droperidol Injectable Sterile Solution Recalled by Premier Pharmacy Labs Inc...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Brilliant Blue Ophthalmic PF INJ Recalled by Premier Pharmacy Labs Inc Due...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Neostigmine Methylsulfate Recalled by Premier Pharmacy Labs Inc Due to Lack...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: SUCCINYLcholine Chloride Recalled by Premier Pharmacy Labs Inc Due to Lack...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: SUCCINYLcholine Chloride Recalled by Premier Pharmacy Labs Inc Due to Lack...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Isoproterenol HCL in D5W (Non Sterile to Sterile) Recalled by Premier...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Sodium Bicarbonate INJ 8.4% Recalled by Premier Pharmacy Labs Inc Due to...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund